ClinVar Miner

List of variants in gene VCL reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_003373.4(VCL):c.*990_*991dup rs397804906
NM_014000.2(VCL):c.*1203A>C rs149551128
NM_014000.2(VCL):c.*292G>C rs77295081
NM_014000.3(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.3(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.3(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.3(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.3(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.3(VCL):c.945C>A (p.Gly315=) rs61731180

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.